Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
CRP Rapid Quantitative Test
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06933260208487
- Basic UDI-DI Code
- B-06933260208487
- Reference
- BT2302
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Xiamen Biotime Biotechnology Co., Ltd.
Additional Description
The Biotime CRP Rapid Quantitative Test is intended to quantify the concentration of CRP, including high-sensitivity CRP(hsCRP) and normal CRP in human serum, plasma or whole blood on Biotime FIA Analyzers by fluorescent immunoasay. The test is used as an aid detection of infectious processes, hsCRP is also used as an aid detection of cardiovascular disease.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102160601 | C-REACTIVE PROTEIN - RT & POC |
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